REACTION OF N-ACYL-ALPHA-METHOXYAMINES WITH ORGANOZINC REAGENTS - CONVENIENT METHOD FOR THE SYNTHESIS OF HOMOALLYLAMINES AND BETA-AMINO ESTERS

被引：27

作者：

KISE, N

YAMAZAKI, H

MABUCHI, T

SHONO, T

机构：

[1] Division of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Yoshida, Sakyo, Kyoto

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 10期

关键词：

D O I：

10.1016/S0040-4039(00)76758-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of N-acyl-alpha-methoxyamines with allyl-, propargyl-, and benzylzinc bromides and Reformatsky reagents proceeds in THF at room temperature. Homoallyl- and homopropargylamines and beta-amino esters are synthesized in good yields.

引用

页码：1561 / 1564

页数：4

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